This study assessed the accuracy of the HEART, EDACS, and simplified EDACS risk scores in predicting major adverse cardiac events (MACE) among 118,822 emergency department patients evaluated for possible acute coronary syndrome (ACS). The study found that using a cardiac troponin I cutoff below the 99th percentile (0.02 ng/ml) optimized the accuracy of all three risk scores, maintaining high negative predictive values around 99.5% for predicting 60-day MACE while improving risk reclassification. The original EDACS identified the largest proportion (60.6%) of patients as low risk. Therefore, the original EDACS may be the preferred risk score for identifying low-risk patients when using a troponin I
Compliance of pharmacological treatment for non-ST-elevation acute coronary syndromes with contemporary guidelines: influence on outcomes
Authors: Hélder Dores, Carlos Aguiar, Jorge Ferreira, Jorge Mimoso, Sílvia Monteiro, Filipe Seixo, José Ferreira Santos, On behalf of Portuguese Registry on Acute Coronary Syndromes (ProACS) Investigators
Improved diagnosis and prognosis using Decisions Informed by Combining Entities (DICE): results from the NHLBI-sponsored Women’s Ischemia Syndrome Evaluation (WISE)
Authors: Mark Doyle, Gerald M. Pohost, C. Noel Bairey Merz, Leslee J. Shaw, George Sopko, William J. Rogers, Barry L. Sharaf, Carl J. Pepine, Diane A. Vido-Thompson, Geetha Rayarao, Lindsey Tauxe, Sheryl F. Kelsey, Douglas Mc Nair, Robert W. Biederman
http://www.ncbi.nlm.nih.gov/pubmed/24400205
http://www.thecdt.org/article/view/3004
Predictive value of exercise myocardial perfusion imaging in the Medicare population: the impact of the ability to exercise
Authors: Deborah H. Kwon, Venu Menon, Penny Houghtaling, Elizabeth Lieber, Richard C. Brunken, Manuel D. Cerqueira, Wael A. Jaber
Serum Uric Acid and Outcome after Acute Ischemic Stroke: PREMIER StudyErwin Chiquete, MD, PhD
Background: Current evidence shows that uric acid is a potent
antioxidant whose serum concentration increases rapidly
after acute ischemic stroke (AIS). Nevertheless, the relationship
between serum uric acid (SUA) levels and AIS
outcome remains debatable. We aimed to describe the
prognostic significance of SUA in AIS. Methods: We studied
463 patients (52% men, mean age 68 years, 13% with glomerular
filtration rate <60 />2) at 30 days, or with
any outcome measure at 3, 6 or 12 months poststroke. After
adjustment for age, gender, stroke type and severity (NIHSS
<9),><24 h. Conclusions: A low SUA
concentration is modestly associated with a very good
short-term outcome. Our findings support the hypothesis
that SUA is more a marker of the magnitude of the cerebral
infarction than an independent predictor of stroke outcome.
Compliance of pharmacological treatment for non-ST-elevation acute coronary syndromes with contemporary guidelines: influence on outcomes
Authors: Hélder Dores, Carlos Aguiar, Jorge Ferreira, Jorge Mimoso, Sílvia Monteiro, Filipe Seixo, José Ferreira Santos, On behalf of Portuguese Registry on Acute Coronary Syndromes (ProACS) Investigators
Improved diagnosis and prognosis using Decisions Informed by Combining Entities (DICE): results from the NHLBI-sponsored Women’s Ischemia Syndrome Evaluation (WISE)
Authors: Mark Doyle, Gerald M. Pohost, C. Noel Bairey Merz, Leslee J. Shaw, George Sopko, William J. Rogers, Barry L. Sharaf, Carl J. Pepine, Diane A. Vido-Thompson, Geetha Rayarao, Lindsey Tauxe, Sheryl F. Kelsey, Douglas Mc Nair, Robert W. Biederman
http://www.ncbi.nlm.nih.gov/pubmed/24400205
http://www.thecdt.org/article/view/3004
Predictive value of exercise myocardial perfusion imaging in the Medicare population: the impact of the ability to exercise
Authors: Deborah H. Kwon, Venu Menon, Penny Houghtaling, Elizabeth Lieber, Richard C. Brunken, Manuel D. Cerqueira, Wael A. Jaber
Serum Uric Acid and Outcome after Acute Ischemic Stroke: PREMIER StudyErwin Chiquete, MD, PhD
Background: Current evidence shows that uric acid is a potent
antioxidant whose serum concentration increases rapidly
after acute ischemic stroke (AIS). Nevertheless, the relationship
between serum uric acid (SUA) levels and AIS
outcome remains debatable. We aimed to describe the
prognostic significance of SUA in AIS. Methods: We studied
463 patients (52% men, mean age 68 years, 13% with glomerular
filtration rate <60 />2) at 30 days, or with
any outcome measure at 3, 6 or 12 months poststroke. After
adjustment for age, gender, stroke type and severity (NIHSS
<9),><24 h. Conclusions: A low SUA
concentration is modestly associated with a very good
short-term outcome. Our findings support the hypothesis
that SUA is more a marker of the magnitude of the cerebral
infarction than an independent predictor of stroke outcome.
Irina Gontschar and Igor Prudyvus
Abstract
Introduction: The purpose of the study is to provide information about the database of 1421 adult patients with acute ischemic stroke (IS) developing ≤ 48 hours before admitting, research methods, study protocol, and clinical predictors of the evolving stroke course (EIS).
Methods and Materials: EIS outlined as an increase of NIHSS ≥ 2 points within seven days or in-hospital lethal outcome. Clinical, demographic, instrumental, laboratory data acquisition, as well as the IS course variant and the functional outcome assessment, were carried out prospectively. Statistical analyses were performed using R V.3.2.5 statistical package software and IBM SPSS Statistics 26.0.
Results: The incidence of EIS reached 30.0%. The average age of patients with EIS was 72.6±10.2 years, compare the age of patients without EIS - 68.1±11.3 years; p = 0.005. Female sex increased the odds of EIS (OR, 1.36; 95% CI 1.08-1.73). Total anterior carotid stroke (OR, 7.78; 95% CI 5.91-10.23), the initial NIHSS score > 14 points (OR, 3.74; 95% CI 2.83-4.94), and the right anterior circulation was also associated with EIS (OR, 1.30; 95% CI 1.02-1.66). The odds of EIS were significantly higher in the presence of diabetes mellitus (OR, 1.29; 95% CI 1.01-1.66), cerebral artery stenosis ≥ 70% (OR, 1.96; 95% CI 1.30-2.93), atrial fibrillation (OR, 1.89; 95% CI 1.51-2.39), congestive heart failure (OR, 1.90; 95% CI 1.51-2.39), and peripheral artery disease (OR, 1.69; 95% CI 1.27-2.25). Respiratory (OR, 2.82; 95% CI 2.22-3.59), gastrointestinal (OR, 1.34; 95% CI 1.05-1.70), and urologic diseases (OR, 2.10; 95% CI 1.65-2.66), stroke-associated infection (OR, 3.47; 95% CI 2.09-5.76), and gradual development of initial IS symptoms before admitting increased the odds of progression of the neurological deficit during treatment (OR, 2.37; 95% CI 1.78-3.15)were associated with the evolving clinical course of IS. The patients with the EIS compared with patients without EIS, showed higher serum levels of glucose (p < 0.001), urea (p = 0.001), creatinine (p < 0.001), sodium (p = 0.025), and direct bilirubin (p = 0.015). Potassium level in EIS group was lower than in the group without EIS (p < 0.001). In patients with EIS, a higher amount of RBC (p = 0.030) and WBC (p < 0.001) was found.
Conclusion: The in-hospital database contains information about EIS by the bases subtypes of IS, patient demography, cardiovascular risk factors, comorbid pathology, clinical and laboratory tests, instrumental methods of examination, medications, the severity of neurological deficit, and post-stroke outcome.
Irina Gontschar and Igor Prudyvus
Abstract
Introduction: The purpose of the study is to provide information about the database of 1421 adult patients with acute ischemic stroke (IS) developing ≤ 48 hours before admitting, research methods, study protocol, and clinical predictors of the evolving stroke course (EIS).
Methods and Materials: EIS outlined as an increase of NIHSS ≥ 2 points within seven days or in-hospital lethal outcome. Clinical, demographic, instrumental, laboratory data acquisition, as well as the IS course variant and the functional outcome assessment, were carried out prospectively. Statistical analyses were performed using R V.3.2.5 statistical package software and IBM SPSS Statistics 26.0.
Results: The incidence of EIS reached 30.0%. The average age of patients with EIS was 72.6±10.2 years, compare the age of patients without EIS - 68.1±11.3 years; p = 0.005. Female sex increased the odds of EIS (OR, 1.36; 95% CI 1.08-1.73). Total anterior carotid stroke (OR, 7.78; 95% CI 5.91-10.23), the initial NIHSS score > 14 points (OR, 3.74; 95% CI 2.83-4.94), and the right anterior circulation was also associated with EIS (OR, 1.30; 95% CI 1.02-1.66). The odds of EIS were significantly higher in the presence of diabetes mellitus (OR, 1.29; 95% CI 1.01-1.66), cerebral artery stenosis ≥ 70% (OR, 1.96; 95% CI 1.30-2.93), atrial fibrillation (OR, 1.89; 95% CI 1.51-2.39), congestive heart failure (OR, 1.90; 95% CI 1.51-2.39), and peripheral artery disease (OR, 1.69; 95% CI 1.27-2.25). Respiratory (OR, 2.82; 95% CI 2.22-3.59), gastrointestinal (OR, 1.34; 95% CI 1.05-1.70), and urologic diseases (OR, 2.10; 95% CI 1.65-2.66), stroke-associated infection (OR, 3.47; 95% CI 2.09-5.76), and gradual development of initial IS symptoms before admitting increased the odds of progression of the neurological deficit during treatment (OR, 2.37; 95% CI 1.78-3.15)were associated with the evolving clinical course of IS. The patients with the EIS compared with patients without EIS, showed higher serum levels of glucose (p < 0.001), urea (p = 0.001), creatinine (p < 0.001), sodium (p = 0.025), and direct bilirubin (p = 0.015). Potassium level in EIS group was lower than in the group without EIS (p < 0.001). In patients with EIS, a higher amount of RBC (p = 0.030) and WBC (p < 0.001) was found.
Conclusion: The in-hospital database contains information about EIS by the bases subtypes of IS, patient demography, cardiovascular risk factors, comorbid pathology, clinical and laboratory tests, instrumental methods of examination, medications, the severity of neurological deficit, and post-stroke outcome.
Coronary heart disease is best addressed by a comprehensive approach aimed at halting atherosclerotic disease and reducing the risk of thrombosis. Unfortunately, our success in optimal risk factor modification in patients with stable CHD remains poor: only 41% of patients achieved all basic goals in the recent ISCHEMIA trial, with success rates likely even lower outside the rigorous clinical trial context. A greater focus on achieving prevention goals in patients with CHD will have a substantial impact on patient outcome and rates of hospitalization and more resources and incentives should be allocated for improved secondary prevention.
The ISCHEMIA trial suggests that even selected, high-risk patients with extensive ischemic burden do not benefit from revascularization barring unacceptable angina despite OMT. As ISCHEMIA excluded patients with unacceptable angina, advanced heart failure, and those with unprotected left main disease, our evaluation may be geared to identify such patients for consideration of revascularization alongside an initial strategy of OMT.
Atherosclerosis is a systemic disease of the arterial circulation, with focal areas of more severe manifestation. From an imaging standpoint, the paradigm of ischemia testing may have come to an end. Recent evidence from COURAGE, PROMISE, SCOT-HEART, and ISCHEMIA has demonstrated that functional testing for inducible myocardial ischemia is inferior to anatomic assessment for risk stratifying and managing patients with suspected or known CHD. Consistent with a large body of evidence, risk from CHD is mediated by the extent of atherosclerotic disease burden and not by the extent of inducible ischemia. Given that 55% of patients had nonobstructive CHD by CT in PROMISE, which was associated with 77% of cardiovascular deaths and myocardial infarctions at follow-up, there is immense opportunity to impact the disease at an earlier stage in a very large population of patients with occult CHD.
Elevated Tissue Doppler E/E' on Index Admission Can Help Identify Patients at...crimsonpublishersOJCHD
Readmissions for congestive Heart Failure (CHF) are a major healthcare problem that contributes significantly to the overall healthcare expenditure. About 24% of patients are readmitted to the hospital within 30 days of discharge. We investigated whether a non-invasive estimate of left atrial filling pressure, an elevated ratio of early trans mitral flow velocity to early diastolic mitral annular velocity (E/E'), during the index admission for CHF could independently predict 30 day readmission.
Cerebral Venous Thrombosis in a Mexican Multicenter Registry of Acute Cerebro...Erwin Chiquete, MD, PhD
Background: Cerebral venous thrombosis (CVT) is a rare form of cerebrovascular
disease that is usually not mentioned in multicenter registries on all-type acute
stroke. We aimed to describe the experience on hospitalized patients with CVT in
a Mexican multicenter registry on acute cerebrovascular disease. Methods: CVT
patients were selected from the RENAMEVASC registry, which was conducted
between 2002 and 2004 in 25 Mexican hospitals. Risk factors, neuroimaging,
and 30-day outcome as assessed by the modified Rankin scale (mRS) were analyzed.
Results: Among 2000 all-type acute stroke patients, 59 (3%; 95% CI, 2.3-3.8%) had
CVT (50 women; female:male ratio, 5:1; median age, 31 years). Puerperium (42%),
contraceptive use (18%), and pregnancy (12%) were the main risk factors in women.
In 67% of men, CVTwas registered as idiopathic, but thrombophilia assessment was
suboptimal. Longitudinal superior sinus was the most frequent thrombosis location
(78%). Extensive (.5 cm) venous infarction occurred in 36% of patients. Only 81% of
patients received anticoagulation since the acute phase, and 3% needed decompressive
craniectomy. Mechanical ventilation (13.6%), pneumonia (10.2%) and systemic
thromboembolism (8.5%) were the main in-hospital complications. The 30-day case
fatality rate was 3% (2 patients; 95% CI, 0.23-12.2%). In a Cox proportional hazards
model, only age ,40 years was associated with a mRS score of 0 to 2 (functional independence;
rate ratio, 3.46; 95% CI, 1.34-8.92). Conclusions: The relative frequency
of CVT and the associated in-hospital complications were higher than in other registries.
Thrombophilia assessment and acute treatment was suboptimal. Young age
is the main determinant of a good short-term outcome.
DANISH is a major breakthrough trial published in NEJM on 29/09/2016 regarding Defibrillator Implantation in Patients with Nonischemic Systolic Heart Failure. All content of this slide is Copy right of NEJM.
Prognosis of Invasive Micropapillary Carcinoma of the Breast Analyzed by Usin...daranisaha
Invasive micropapillary carcinoma (IMPC) is a rare type of breast cancer with high frequency of regional lymph node metastasis. However, the prognosis of IMPC has remained controversial for decades. We aimed to compare the differences of prognosis between IMPC and Invasive ductal carcinoma(IDC) of the breast by utilizing Surveillance, Epidemiology, and End Results (SEER) database.
Prognosis of Invasive Micropapillary Carcinoma of the Breast Analyzed by Usin...eshaasini
Invasive micropapillary carcinoma (IMPC) is a rare type of breast cancer with high frequency of regional lymph node metastasis. However, the prognosis of IMPC has remained controversial for decades. We aimed to compare the differences of prognosis between IMPC and Invasive ductal carcinoma(IDC) of the breast by utilizing Surveillance, Epidemiology, and End Results (SEER) database
Prognosis of Invasive Micropapillary Carcinoma of the Breast Analyzed by Usin...semualkaira
Invasive micropapillary carcinoma (IMPC) is a rare type of breast cancer with high frequency of regional lymph node metastasis. However, the prognosis of IMPC has remained controversial for decades. We aimed to compare the differences of prognosis between IMPC and Invasive ductal carcinoma(IDC) of the breast by utilizing Surveillance, Epidemiology, and End Results (SEER) database.
Prognosis of Invasive Micropapillary Carcinoma of the Breast Analyzed by Usin...semualkaira
Invasive micropapillary carcinoma (IMPC) is a rare type of breast cancer with high frequency of regional lymph node metastasis. However, the prognosis of IMPC has remained controversial for decades. We aimed to compare the differences of prognosis between IMPC and Invasive ductal carcinoma(IDC) of the breast by utilizing Surveillance, Epidemiology, and End Results (SEER) database.
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
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New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
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These lecture slides, by Dr Sidra Arshad, offer a quick overview of physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
Acute scrotum is a general term referring to an emergency condition affecting the contents or the wall of the scrotum.
There are a number of conditions that present acutely, predominantly with pain and/or swelling
A careful and detailed history and examination, and in some cases, investigations allow differentiation between these diagnoses. A prompt diagnosis is essential as the patient may require urgent surgical intervention
Testicular torsion refers to twisting of the spermatic cord, causing ischaemia of the testicle.
Testicular torsion results from inadequate fixation of the testis to the tunica vaginalis producing ischemia from reduced arterial inflow and venous outflow obstruction.
The prevalence of testicular torsion in adult patients hospitalized with acute scrotal pain is approximately 25 to 50 percent
2. hospital discharge (4,5). However, among those
without diagnostic electrocardiograms (ECGs) and/or
cardiac biomarkers, only 1% to 4% of these patients
have angiographic evidence of significant coronary
artery disease (6–8).
Given the relatively low yield of this historic
approach to possible ACS, researchers have created
risk scores to identify patients at low risk of major
adverse cardiac events (MACE). Among these, the
modified History, Electrocardiogram, Age, Risk fac-
tors and Troponin (HEART) score and the Emergency
Department Assessment of Chest pain Score (EDACS),
both of which treat abnormal troponin values as in-
dependent, non–low-risk factors, stand out with the
best specificities (ranging from 40% to 60%) in
achieving negative predictive value (NPV) estimates
>99% for 30- to 45-day MACE, specifically when
applied alongside accelerated diagnostic protocols
employing cardiac troponin I (cTnI) measurement at
ED arrival and 2 to 3 h later (9–12). Used in this
fashion, both scores have demonstrated improve-
ments in operational efficiency and downstream
resource utilization (10,12). A simplified unweighted
version of the EDACS, which has minimal reliance on
presenting symptoms, performs similarly well in
terms of NPV, albeit with lower specificity (13).
The use of these risk scores may allow for direct
discharge of patients with possible ACS from the ED
without further planned cardiac testing, an approach
that appears safe, medico-legally acceptable to cli-
nicians, and cost-effective (12,14–17). However,
adoption in practice is limited by imprecision in
risk estimates, as well as uncertainty surrounding
the optimal cTnI cutoff, given increased risks of
future MACE among patients with cTnI concentra-
tions at the high end of the normal range (18–21).
Accordingly, we sought to improve both the preci-
sion and accuracy of risk estimates by exploring the
incorporation of alternative cutoffs for cTnI below
the 99th percentile among a large retrospective
cohort drawn from the electronic health record of an
integrated health system. We contextualized our
analysis and findings from a risk-benefit perspective
using estimated testing thresholds for functional or
anatomic testing in patients with possible ACS,
supported by cost-benefit estimates (14,22). We hy-
pothesized that improved accuracy and precision in
risk estimates could identify a sizeable portion of ED
patients with possible ACS for whom routine func-
tional or anatomic testing is unlikely beneficial
(8,22–25).
METHODS
STUDY DESIGN, SETTING, AND SUBJECTS.
We conducted a retrospective study of pa-
tients with ED visits between January 1, 2013,
and December 31, 2015, to the 21 medical
centers within Kaiser Permanente Northern
California, a private, not-for-profit integrated
health system of 3.8 million members
covering approximately 33% of the region’s
insured population. The Kaiser Permanente
Northern California Institutional Review
Board approved the study. All arenas of care
(inpatient, outpatient, emergency) within the
system utilize a single integrated electronic
health record (Epic, Verona, Wisconsin),
including all clinical documentation and
comprehensive pharmacy, laboratory, and
imaging data.
Study inclusion criteria were age >17 years,
cTnI testing during the index ED visit, and either of
the following: a chief complaint of chest pain or chest
discomfort, or a primary or second position Interna-
tional Statistical Classification of Diseases and
Related Health Problems-9th revision (ICD-9) or 10th
revision (ICD-10) coded diagnosis of chest pain by the
treating ED physician. For consistent capture of out-
comes, continuous health system insurance coverage
status was required in the month of the index visit as
well as the 2 months following, unless interrupted by
death. Patients were excluded if they had a diagnosis
of myocardial infarction, cardiac arrest, or cardio-
genic shock in the ED or 30 days before, or if they had
a cTnI concentration above the 99th percentile in the
ED. Patients were also excluded if they had certain
chest pain–related diagnoses during the index hos-
pitalization (Online Table 1). Only the first qualifying
visit for any given patient during the study period
was included.
cTnI values at all sites were obtained using the
Access AccuTnI assay (Beckman-Coulter, Brea, Cali-
fornia) from the beginning of the study period
through July 14, 2014, and then using the Access
AccuTnIþ3 assay (Beckman-Coulter, Brea, California)
from July 15, 2014, through the end of the study
period. The 99th percentile for both assays is
0.04 ng/ml per local institutional reporting guidelines
and reference published reports (26). In terms of
imprecision, the coefficient of variation at a concen-
tration of 0.04 ng/ml is 14% and 10% for the Access
AccuTnI and Access AccuTnIþ3, respectively; at
0.02 ng/ml, it is 20% for both assays, making
0.02 ng/ml the lowest acceptable cutoff value
for the exclusion of myocardial infarction (limit of
SEE PAGE 617
A B B R E V I A T I O N S
A N D A C R O N Y M S
ACS = acute coronary
syndrome
CI = confidence interval
cTnI = cardiac troponin I
ECG = electrocardiogram
ED = emergency department
EDACS = Emergency
Department Assessment of
Chest pain Score
HEART = History,
Electrocardiogram, Age, Risk
factors and Troponin
ICD = International
Classification of Disease
MACE = major adverse cardiac
event
NPV = negative predictive
value
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F E B R U A R Y 1 3 , 2 0 1 8 : 6 0 6 – 1 6 Comparing the EDACS and Modified HEART Score
607
3. quantitation) (27). The limits of blank and detection
for both assays are <0.01 ng/ml and 0.01 ng/ml,
respectively.
DATA COLLECTION AND OUTCOME MEASURES. To
identify predictor variables for the risk score calcu-
lations (Table 1), we used a combination of electronic
extraction of structured data (Online Table 2) and text
string processing of unstructured clinical notes and
ECG interpretations from the index ED encounter
(Online Appendix). Using an iterative process, we
developed text string algorithms that categorized key
elements of the presenting symptoms as either “pre-
sent,” “absent,” or “missing data.” Text string
searches were also used to supplement smoking sta-
tus and family history of premature coronary artery
disease, as well as to categorize final ECG in-
terpretations as ischemic, nonspecific, or normal. Six
investigators manually abstracted risk score predictor
variables from a random sample of 450 charts to
calculate measures of agreement for the individual
text string algorithms.
The primary outcome of interest was the cumula-
tive 60-day MACE rate, defined as the composite
outcome of myocardial infarction, cardiac arrest,
cardiogenic shock, and all-cause mortality. A MACE
was considered to have occurred if a corresponding
ICD code was the first or second diagnosis listed at an
TABLE 1 Modified HEART, Original EDACS, and Simplified EDACS
Scores: Data Elements and Weights
HEART variables (modified for retrospective review)
Low risk 0–3 points; Non-low risk $4 points
History
Typical symptoms
- Exertional chest pain or dyspnea; pain radiating to arm,
shoulder, neck or jaw; diaphoresis
Atypical symptoms
- Pain worse with inspiration; pain reproduced by palpation
Typical symptoms only (highly suspicious, 2 points)
Both typical and atypical symptoms, (moderately suspicious,
1 point)
Only atypical symptoms (slightly suspicious, 0 points)
Electrocardiogram findings
Ischemia (2 points)
Nonspecific abnormalities (i.e., fascicular blocks, 1 point)
Normal (0 points)
Age
>65 (2 points)
45–65 (1 point)
#45 (0 points)
Risk factors (hypercholesterolemia, hypertension, diabetes, smoking in
past 90 days, premature family history of premature coronary
artery disease in 1st-degree relative <55 years of age, body
mass index $30)
3 risk factors OR any known atherosclerotic disease (coronary
revascularization, cerebrovascular accident, myocardial
infarction, peripheral artery disease; 2 points)
1–2 risk factors (1 point)
0 risk factors (0 points)
Original EDACS variables
Low risk 0–15 points; Non-low risk ‡16 points
Age
18–45 (2 points)
46–50 (4 points)
51–55 (6 points)
56–60 (8 points)
61–65 (10 points)
66–70 (12 points)
71–75 (14 points)
76–80 (16 points)
81–85 (18 points)
86þ (20 points)
Known coronary artery disease (previous myocardial infarction,
coronary bypass surgery or percutaneous coronary
intervention) OR $3 cardiac risk factors in patients age #50
years (4 points)
Premature family history of premature coronary artery disease in
1st-degree relative (age <55 years)
Hyperlipidemia
Diabetes
Smoking within past 90 days
Hypertension
Male sex (6 points)
Typical symptoms
Diaphoresis (3 points)
Pain radiating to arm, shoulder, neck or jaw (5 points)
Atypical symptoms
Pain with inspiration (subtract 4 points)
Pain reproduced by palpation (subtract 6 points)
Continued in the next column
TABLE 1 Continued
Simplified unweighted EDACS score
Low risk 0–3 points; Non-low risk ‡4 points
Age
18–39 (0 points)
40–49 (1 point)
50–59 (2 points)
60–69 (3 points)
70–79 (4 points)
80–89 (5 points)
90þ (6 points)
Known coronary artery disease (previous myocardial infarction,
coronary bypass surgery or percutaneous coronary
intervention) OR $3 cardiac risk factors in patients aged #50
years (1 point)
Premature family history of premature coronary artery disease in
1st-degree relative (age <55 years)
Hyperlipidemia
Diabetes
Smoking within past 90 days
Hypertension
Male sex (1 point)
Symptoms
Pain radiating to arm, shoulder, neck or jaw (1 point)
EDACS ¼ Emergency Department Assessment of Chest pain Score;
HEART ¼ History, Electrocardiography, Age, Risk Factors, Troponin.
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4. inpatient or subsequent ED encounter within the in-
tegrated health system. Additionally, we queried
claims for services provided at facilities outside of the
study setting without regard for coding position. The
secondary endpoint was MACE inclusive of either
percutaneous or surgical coronary revascularization
(MACE plus). Revascularization was not included de
facto in the primary composite outcome due to the
inability to categorize these procedures as either
emergent or elective, the latter of which would be
inconsistent with consensus agreements on appro-
priate MACE endpoints (28). Mortality was deter-
mined using a composite death database of internal
health system mortality statistics cross-referenced
with state (California death index) and federal (so-
cial security death index) data. Finally, we collected
measures of resource utilization, including ED length
of stay, rates of inpatient or observation status
admission, and 30-day downstream use of functional
or anatomic cardiac testing. Outcome and utilization
coding details are provided in Online Table 3.
RISK SCORE CALCULATION AND RESULT REPORTING. The
modified HEART, original EDACS, and simplified
EDACS scores were calculated for each eligible pa-
tient, assigning points as per Table 1, with the his-
tory component of the modified HEART score
calculated as described in the Online Appendix
(12,13). We dichotomized each score into low-risk
and non–low-risk categories using previously re-
ported cutoffs, with non–low-risk designation indi-
cated by a modified HEART score $4, an original
EDACS $16 or a simplified EDACS $4 (9,12,13). We
also further stratified populations based on the
highest reported cTnI values (below the 99th
percentile) during the ED evaluation. Finally, given
published sex- and age-specific differences in the
99th percentile for cTnI, we also assessed stratifi-
cation on these variables (26,29). Time-to-event
curves were generated to compare MACE rates be-
tween identified risk strata. Analysis was performed
using SAS version 9.3 (SAS institute, Cary, North
Carolina).
Because, in terms of disposition decision making,
ED physicians are primarily concerned with the pos-
terior probability of disease among patients with
undifferentiated chest pain, we reported test char-
acteristics for the low-risk categories of each respec-
tive risk score in terms of either the NPV or outcome
rate per 1,000 patients. We elected not to report
sensitivity and specificity because we excluded pa-
tients with either cTnI concentrations above the 99th
percentile or a MACE diagnosis in the ED, recognizing
that the resulting lower overall acuity and prevalence
of disease will result in lower test sensitivities and
higher specificities (spectrum effect), potentially
causing unnecessary confusion (30).
RECLASSIFICATION YIELD. To quantitatively sum-
marize differences in accuracy among the 3 risk
scores, as well as between alternative cTnI thresh-
olds, we reported the net increase in true positives
(patients with a MACE reclassified as non-low risk)
and the net increase in false positives (patients
without a MACE reclassified as non-low risk) as a
proportion (net increase in true positives over the
sum of the net increase in both true and false posi-
tives), which we term the “reclassification yield.”
This allows for an estimate of the event rate among
the sum of patients reclassified as non-low risk,
which can then be directly compared to a test
threshold to determine whether the reclassification
scheme was beneficial. We calculated test thresholds
using the methods of Pauker and Kassirer (22) with
risk-benefit estimates from the available published
reports (8,31–35), resulting in testing threshold esti-
mates between 0.71% and 0.91%, below which the
risks of false-positive testing are outweighed by the
potential for harm from untreated disease (36). To
simplify interpretation, we designated a reclassifica-
tion yield of >1% as clinically significant. To alterna-
tively contextualize these testing thresholds, we also
extrapolated cost-effectiveness data (14) for exercise
treadmill testing and computed tomography coronary
angiography, which yielded cost estimates in excess
of $100,000 per quality-adjusted life-year gained.
Details of these calculations are provided in the
Online Appendix.
SENSITIVITY ANALYSES. We conducted 8 sensitivity
analyses by altering the inclusion, exclusion, and
outcome criteria for the cohort (Online Appendix).
These analyses were meant to provide a broader
range of 60-day MACE and MACE plus estimates by
removing certain assumptions (e.g., including pa-
tients with comorbid chest pain-related exclusion
diagnoses), as well as to examine narrower pop-
ulations (e.g., patients with 2 or more cTnI measure-
ments in the ED).
RESULTS
From a total of 3,267,915 encounters within the 21 EDs
of the Kaiser Permanente Northern California inte-
grated health system during the study period, among
those undergoing cTnI testing in the ED, there were a
total of 172,304 adult patients (5.27%) who presented
with a chief complaint of chest pain or chest
discomfort, and a total of 112,691 patients (3.45%)
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609
5. who were given a primary or second position ICD-
coded diagnosis of chest pain by their ED physician,
resulting in 188,310 (5.76%) unique patient encoun-
ters, of which 8.0% had a known 60-day MACE.
Exclusion criteria left a total of 118,822 patients with
possible ACS for analysis in the study cohort. A
CONSORT diagram of the cohort selection is pre-
sented in Figure 1.
The demographic characteristics of the study
cohort are presented in Table 2. The median age was
59 years, 42.70% were male, and 9.88% were hospi-
talized at the index ED encounter. The overall 60-day
MACE rate was 1.94%, whereas the overall 60-day
MACE plus rate was 3.69%. Follow-up cardiac
testing (functional or anatomic) was requested for
41.50% of all patients within the next 30 days.
Analysis stratified by varying cTnI cutoffs revealed
a clinically significant reclassification yield (i.e., >1%)
only at the transition between a cTnI concentration
of <0.02 ng/ml (lower limit of quantitation) and
0.02 ng/ml, a finding that persisted regardless of sex
or age strata (Online Tables 4 and 5). When applied to
the 3 risk scores, using a lower cTnI cutoff
of <0.02 ng/ml, as compared with the 99th percentile
(0.04 ng/ml), resulted in reclassification yields
ranging from 3.40% to 3.93%, indicating clinically
important improvements in accuracy (Table 3).
Accordingly, the NPVs for the risk scores were lower
for 60-day MACE (range: 99.49% to 99.55% vs. 99.19%
to 99.32%) and 60-day MACE plus (range: 98.88% to
99.08% vs. 98.37% to 98.75%), with the original
EDACS identifying the largest proportion of patients
as low risk (60.6%; 95% confidence interval [CI]:
60.3% to 60.9%) as compared with the modified
HEART (51.8%; 95% CI: 51.6% to 52.1%) or the
simplified EDACS (48.1%; 95% CI: 47.8% to 48.3%;
p < 0.0001) (Table 4).
Building upon these data, we conceptualized 4
strata of risk among patients with possible ACS by
combining risk scores with dichotomized peak ED
cTnI concentrations within the 99th percentile
(<0.02 ng/ml vs. 0.02 to 0.04 ng/ml), graphically
represented for each risk score with time-to-event
MACE (Figure 2) and MACE plus (Online Figure 1)
FIGURE 1 Study Cohort Selection
• MACE diagnosis in ED (n = 5,400)
• MACE diagnosis in 30 days prior to ED visit
(n = 2,874)
• Alternative non-ACS diagnoses at index ED
visit or admission* (n = 29,472)
• No active health plan membership in
month of the index ED visit and two
months following, except in cases of death
(n = 22,863)
• Troponin I result >0.04 ng/ml (n = 14,706)
Exclusions:
60-day MACE rate 1.9%
60-day MACE rate 8.0%
Primary study cohort (n = 118,822)
• Age ≥18 years
• Troponin I testing during ED visit
Initial cohort (n = 188,310) with either chief complaint of chest pain/discomfort
(n = 172,304) or ICD-coded ED diagnosis of chest pain (n = 112,691), plus:
*Non-ACS diagnoses included pneumonia and other respiratory tract infections, aortic dissection, acute pericarditis, myocarditis or endo-
carditis, pneumothorax, traumatic injuries, or external causes of injury and poisoning. ACS ¼ acute coronary syndrome; ED ¼ emergency
department; EDACS ¼ Emergency Department Assessment of Chest pain Score; HEART ¼ History, Electrocardiogram, Age, Risk factors and
Troponin; ICD ¼ international classification of diseases; MACE ¼ major adverse cardiac event (composite of acute myocardial infarction,
cardiac arrest, cardiogenic shock and all-cause mortality).
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Comparing the EDACS and Modified HEART Score F E B R U A R Y 1 3 , 2 0 1 8 : 6 0 6 – 1 6
610
6. survival curves. Overall, 8% to 9% of patients with a
low-risk score and 21% to 25% with a non–low-risk
score had peak cTnI concentration in the 0.02 to
0.04 ng/ml range while in the ED, which correlated
with a roughly 5-fold increase in estimated 60-day
MACE rates compared with the same risk score cate-
gory with a peak cTnI concentration of <0.02 ng/ml.
When comparing accuracy between the 3 low-risk
scores for predicting 60-day MACE using a cTnI cut-
off of <0.02 ng/ml (Table 5), moving from the original
EDACS to either the modified HEART score (reclassi-
fication yield: 0.86%; 95% CI: 0.70% to 1.06%) or
the simplified EDACS (reclassification yield: 0.66%;
95% CI: 0.54% to 0.80%) did not result in clinically
significant improvements. However, the simplified
EDACS was inferior when compared to the modified
HEART score (reclassification yield: 0.19%; 95% CI:
0.11% to 0.38%), which is well below the lower testing
threshold estimate of 0.71%.
Sensitivity analyses examining the stability of 60-
day MACE and MACE plus rates per 1,000 patients
among the 4 conceived strata of risk were largely
stable, exceptions being lower event rates when
restricting to patients with 2 or more cTnI measure-
ments during ED evaluation, excluding patients with
MACE diagnoses within the first day of inpatient
admission at the index ED visit, or restricting to pa-
tients with orders for functional or anatomic cardiac
testing. Slightly higher estimates were conversely
observed when including patients with chest pain
related exclusion diagnoses. Detailed results and
accompanying discussion for each sensitivity analysis
are available in the supplementary index (Online
Tables 6 to 9).
Finally, when comparing manually to electroni-
cally abstracted variables, percent agreement and
unweighted kappa values ranged between 94.4% and
98.8%, and 0.77 and 0.91 for individual risk score
variables, respectively, whereas overall dichotomous
risk score classification agreement ranged between
96.9% and 99.3%, and 0.94 and 0.99, respectively,
signifying that significant nonrandom bias in elec-
tronic risk score calculation was highly unlikely
(Online Table 10).
DISCUSSION
In this retrospective study of patients with possible
ACS following an ED evaluation, we found that the
accuracy of a low-risk classification for 60-day MACE
by 3 risk scores (modified HEART, original EDACS,
and simplified EDACS) was optimized using a cTnI
concentration threshold of <0.02 ng/ml (lower limit
of quantitation) (Central Illustration). Of the 3 risk
TABLE 2 Cohort Characteristics (N ¼ 118,822)
Risk factors
Age, yrs 59 (47–71)
Male 42.7
Hypertension 52.5
Hypercholesterolemia 53.5
Diabetes mellitus 24.0
Coronary artery disease 18.8
Coronary revascularization 11.3
Myocardial infarction 11.6
Stroke 9.1
Peripheral artery disease 3.9
Estimated glomerular filtration rate <60 ml/min/1.73 m2
17.1
Smoker in past 90 days 11.2
Family history of premature coronary disease 5.8
Obesity (BMI $30 kg/m2
) 40.9
Red flag initial vital signs (HR >100 or <50 beats/min,
SBP <100 mm Hg, RR >20 breaths/min, SaO2 <95%)
13.1
Symptoms
Diaphoresis 14.2
Radiating pain 28.3
Palpation pain 12.9
Pleuritic pain 14.8
Exertional symptoms 17.0
Sharp or stabbing pain 21.1
Electrocardiogram
Normal 59.1
Nondiagnostic 34.7
Ischemic 4.8
ED disposition
Admission 9.9
Transfer 0.6
Observation unit 11.6
Discharge 76.9
Against medical advice 1.0
Expired <0.001
Length of stay, h 3.8 (2.6–5.5)
Outcomes at 60 days
Diagnosis
Acute myocardial infarction 1.25
Cardiac arrest 0.21
Cardiogenic shock 0.08
Percutaneous coronary intervention 2.08
Coronary artery bypass surgery 0.39
Death 0.82
Composite MACE rate 1.94
Composite MACE plus rate 3.69
Utilization at 30 days
Cardiac test requested
ECG stress treadmill 29.7
Stress myocardial perfusion imaging 12.0
Stress echocardiography 0.7
Computed tomography coronary angiography 0.4
Catheter coronary angiography 4.5
Total composite rate 41.5
Values are median (interquartile range) or %.
BMI ¼ body mass index; ECG ¼ electrocardiogram; ED ¼ emergency department; HR ¼ heart
rate; MACE ¼ major adverse cardiac events (composite of acute myocardial infarction, cardiac
arrest, cardiogenic shock, and all-cause mortality); RR ¼ respiratory rate; SaO2 ¼ oxygen satu-
ration; SBP ¼ systolic blood pressure.
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7. scores, the original EDACS classified the greatest
proportion of patients as low risk and performed
similarly when compared when either the modified
HEART score or the simplified EDACS in terms of
accuracy.
The fact that lowering the cTnI threshold for low-
risk designation below the 99th percentile resulted
in a clinically significant reclassification yield is not
surprising. Indeed, using the 99th percentile may be
a misguided approach to excluding downstream
MACE, because patients with varying levels of car-
diac disease (and MACE risk) are unavoidably pre-
sent in reference populations. As such, a strategy
designed to “rule out” disease will require a lower
determinant threshold as compared with a “rule-in”
strategy. This phenomenon is evident in the fact
that average cTn concentrations are lower than the
99th percentile among similarly aged patients with
minimal rates of long-term cardiac outcomes
(18,20,21). Even for near-horizon events, studies
examining the predictive value of high-sensitivity
cTn in practice have shown that thresholds well
below the 99th percentile and/or a lack of very small
changes in cTn on serial testing offer improved
NPV for 30-day MACE over use of the 99th percentile
(37–39). Other studies have demonstrated that add-
ing clinical risk criteria can reasonably allow the use
of the 99th percentile to exclude short-term out-
comes (10,12,40,41). As such, a combination of the 2
strategies (use of a risk score with a cTn threshold
below the 99th percentile) is likely to offer improved
safety and discrimination for longer-term outcomes,
as suggested by our findings.
Whether further improvements in accuracy can be
obtained using lower cTn thresholds in conjunction
with risk scores remains unclear, but offers an avenue
for further exploration with high sensitivity cTn as-
says (42). Regardless, it is arguable that the levels of
NPV for 60-day MACE observed among the lowest risk
group (low-risk score and cTnI <0.02 ng/ml) are suf-
ficiently low to consider forgoing further evaluation
with functional or anatomic cardiac testing. Indeed,
several observational studies have found a lack of
reduction in downstream MACE when pursuing such
testing among similarly low risk patients (8,23–25). At
the very least, this practice is not likely to be cost-
effective, with estimates in excess of $100,000 per
quality-adjusted life-year when applied to pop-
ulations with MACE rates below 1%, as summarized in
the Online Appendix (14).
Along these lines, in terms of optimizing resource
utilization, the original EDACS may be the preferred
single risk score because it classified the greatest
proportion of patients as low risk. Two prospective
and 2 retrospective validation studies of the original
EDACS yielded similar low-risk proportions among ED
patients with chest pain which, individually or
pooled, also demonstrated NPVs for 30-day MACE
(pooled 95% CI: 99.23% to 99.94%) that overlap the
95% CIs seen in our study, further supporting this
conclusion (9–11,43).
TABLE 3 Reclassification Yield for 60-Day MACE Using a cTnI Cutoff of <0.02 ng/ml
Instead of #0.04 ng/ml
Correctly
Reclassified Patients
Falsely Reclassified
Patients
Reclassification
Yield, % (95% CI)
Modified HEART low risk 176 5,006 3.40 (2.94–3.93)
Original EDACS low risk 275 6,721 3.93 (3.50–4.41)
Simplified EDACS low risk 196 4,853 3.88 (3.38–4.45)
cTnI ¼ cardiac troponin I; other abbreviations as in Tables 1 and 2.
TABLE 4 60-Day Outcomes by Low–Risk-Score Designation Among Patients With a Peak cTnI Level #0.04 ng/ml (99th Percentile)
Versus <0.02 ng/ml (Limit of Quantitation) During Evaluation in the ED
cTnI Cutoff for Low-Risk
Designation
NPV for 60-Day MACE
(95% CI)
NPV for 60-Day MACE Plus
(95% CI)
Number of Patients Meeting
Low-Risk Criteria (%, 95% CI)
#0.04 ng/ml
Modified HEART, low-risk 99.32 (99.25–99.38) 98.75 (98.66–98.83) 66,765 (56.2, 55.9–56.5)
Original EDACS, low-risk 99.19 (99.12–99.25) 98.37 (98.28–98.46) 79,008 (66.5, 66.2–66.8)
Simplified EDACS, low-risk 99.25 (99.18–99.32) 98.41 (98.31–98.51) 62,158 (52.3, 52.0–52.6)
<0.02 ng/ml
Modified HEART, low-risk 99.55 (99.49–99.60) 99.08 (99.01–99.16) 61,583 (51.8, 51.6–52.1)
Original EDACS, low-risk 99.49 (99.44–99.54) 98.88 (98.80–98.95) 72,012 (60.6, 60.3–60.9)
Simplified EDACS, low-risk 99.53 (99.47–99.58) 98.88 (98.79–98.96) 57,109 (48.1, 47.8–48.3)
Chi-square analysis by grouping. For cTnI #0.04: 60-day MACE (p ¼ 0.0012); 60-day MACE plus (p < 0.0001); patients meeting low-risk criteria (p < 0.0001). For
cTnI <0.02 ng/ml: 60-day MACE (p ¼ 0.27), 60-day MACE plus (p ¼ 0.0003); patients meeting low-risk criteria (p < 0.0001).
CI ¼ confidence interval; MACE plus ¼ major adverse cardiac events including coronary revascularization; NPV ¼ negative predictive value; other abbreviations as in Tables 1,
2, and 3.
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8. STUDY LIMITATIONS. First, this study was conducted
within an integrated health system and thus may not
be representative of other ED practice environments.
Next is the potential unreliability of retrospectively
assigning a risk score using unstructured clinical
notes. It was primarily for this reason that we
included the simplified EDACS score in our analysis,
because its reliance on symptoms is minimal (only
uses radiation of pain), allowing us to use it as a
control for the original EDACS, given existing data
comparing the relative prospective performance of
the 2 scores (13). It is reassuring that our results were
fully consistent with these prior findings (equivalent
NPV between the 2 scores and a 20% relative decrease
in low-risk proportion using the simplified EDACS).
Also, the retrospective collection of symptom-based
categorical data resulted in missing data, which
were conservatively imputed as absent symptoms.
Similar strategies have been used by other in-
vestigators to retrospectively calculate the original
EDACS and modified HEART scores, with resulting
test characteristics similar to those found in pro-
spective studies (11,44). By considering missingness
as the equivalent of absence, our study is effectively
biased towards misclassifying patients with undocu-
mented typical symptoms as low risk, and conversely
misclassifying patients with undocumented atypical
symptoms as non-low risk. In both cases, the result
should be an overestimation of 60-day MACE rates
among low-risk patients. Accordingly, we can feel
more confident that our NPV estimates for the low-
risk subgroups are, at worst, conservatively low
estimates.
It is also possible that our cohort selection method
resulted in dilution of the sample with patients whose
clinicians did not truly have concern for ACS (spec-
trum bias). To assess for this possibility, we restricted
the analysis to patients with either 2 cTnI measure-
ments in the ED (sensitivity analysis S2), or orders for
functional or anatomic cardiac tests within 30 days
(sensitivity analysis S8) as potential surrogate
markers for higher clinical concern. We found that the
MACE rates in both these groups were up to 2-fold
lower than the primary cohort, arguing against such
a bias. The lower MACE rate among the S2 group may
be due to expedited hospital admission without serial
cTnI testing in the ED among patients who later ruled
in for ACS, as suggested by similar MACE rates in the
S5 analysis, which excluded patients with a MACE
within 1 day of hospital admission at the index visit.
At the same time, ED clinicians may have further
selected out lower-risk patients through the use of
serial cTnI testing. Together, these findings support
FIGURE 2 Time to MACE, Stratified by Risk Category and
cTnI Concentration
NegativePredictiveValue
0.96
1.00
0.92
0.88
0.84
0 60504030
Days to Event
Days to Event
Negative Predictive Value for MACE, Modified HEART
20
Low Risk Score, cTnl <0.02 ng/ml (n = 61,583)
Non-Low Risk Score, cTnl <0.02 ng/ml (n = 40,077)
Low Risk Score, cTnl 0.02-0.04 ng/ml (n = 5,182)
Non-Low Risk Score, cTnl 0.02-0.04 ng/ml (n = 11,980)
10
A
Low Risk Score, cTnl <0.02 ng/ml (n = 57,109)
Non-Low Risk Score, cTnl <0.02 ng/ml (n = 44,551)
Low Risk Score, cTnl 0.02-0.04 ng/ml (n = 5,049)
Non-Low Risk Score, cTnl 0.02-0.04 ng/ml (n = 12,113)
NegativePredictiveValue
0.96
1.00
0.92
0.88
0.84
0 60504030
Days to Event
Negative Predictive Value for MACE, Simplified EDACS
2010
C
Low Risk Score, cTnl <0.02 ng/ml (n = 72,012)
Non-Low Risk Score, cTnl <0.02 ng/ml (n = 29,648)
Low Risk Score, cTnl 0.02-0.04 ng/ml (n = 6,996)
Non-Low Risk Score, cTnl 0.02-0.04 ng/ml (n = 10,166)
NegativePredictiveValue
0.96
1.00
0.92
0.88
0.84
0 60504030
Negative Predictive Value for MACE, Original EDACS
2010
B
The lighter upper and lower lines indicate 95% confidence intervals.
cTnI ¼ cardiac troponin I; other abbreviations as in Figure 1.
J A C C V O L . 7 1 , N O . 6 , 2 0 1 8 Mark et al.
F E B R U A R Y 1 3 , 2 0 1 8 : 6 0 6 – 1 6 Comparing the EDACS and Modified HEART Score
613
9. recommendations to perform serial and/or appropri-
ately delayed cTn testing in the ED, as was done in
the modified HEART pathway and EDACS accelerated
diagnostic protocol studies (9,10,12).
It should also be noted that the 2 most recent
studies of the EDACS added “red flag” criteria (cre-
scendo angina or abnormal vital signs) as stand-
alone, non–low-risk criteria, irrespective of the risk
score, in order to reach NPV point estimates of 100%
(10,11). Although we were unable to fully evaluate the
impact of these additional criteria given limitations in
assessing for crescendo angina retrospectively, we
intentionally did not include vital signs in our pri-
mary validation analysis because these were not
found to improve diagnostic accuracy in the deriva-
tion of the EDACS (9). Regardless, the NPV estimates
found in the lowest-risk group need not be 100% to
justify forgoing further testing, as discussed in the
preceding text.
CONCLUSIONS
Among ED patients with possible ACS, either the
modified HEART score, the original EDACS or the
simplified EDACS were accurate in predicting a
low risk of 60-day MACE (i.e., >99% NPV), with
the original EDACS classifying the greatest pro-
portion of patients as low-risk. Accuracy was
TABLE 5 Reclassification Yield for 60-Day MACE Between Low-Risk Scores Among
Patients With Peak cTnI <0.02 ng/ml
Correctly
Reclassified Patients
Falsely
Reclassified
Patients
Reclassification
Yield (%)
Original EDACS to modified HEART 90 10,339 0.86 (0.70–1.06)
Original EDACS to simplified EDACS 99 14,804 0.66 (0.54–0.80)
Modified HEART to simplified EDACS 9 4,465 0.19 (0.11–0.38)
Abbreviations as in Tables 1 to 3.
CENTRAL ILLUSTRATION Performance of the EDACS Versus Modified HEART Score Among Emergency
Department Patients With Chest Pain
60
cTnl <0.02 + LOW RISK SCORE
cTnl <0.02 + NON-LOW RISK SCORE
cTnl 0.02-0.04 + LOW RISK SCORE
cTnl 0.02-0.04 + NON-LOW RISK SCORE
30701.00
0.95
NPV
DAYS
0.90
Lower troponin cut-off to define low risk is superior
EDACS & mHEART perform similarly in terms of NPV
mHEART
NPV
99.5
EDACS
NPV
99.5
EDACS categorizes more patients as low risk
EDACS mHEART
60.6%
LOW RISK
51.8%
LOW RISK
Mark, D.G. et al. J Am Coll Cardiol. 2018;71(6):606–16.
The EDACS and mHEART scores provide equivalent NPVs for cardiac events. EDACS classifies more patients as low risk. Risk stratification is improved using a cTnI cutoff
below the 99th percentile. cTnI ¼ cardiac troponin I; EDACS ¼ Emergency Department Assessment of Chest pain Score; HEART ¼ History, Electrocardiogram, Age,
Risk factors and Troponin; mHEART ¼ modified History, Electrocardiogram, Age, Risk factors and Troponin; NPV ¼ negative predictive value.
Mark et al. J A C C V O L . 7 1 , N O . 6 , 2 0 1 8
Comparing the EDACS and Modified HEART Score F E B R U A R Y 1 3 , 2 0 1 8 : 6 0 6 – 1 6
614
10. optimized by lowering the cTnI cutoff to the lower
limit of quantitation (<0.02 ng/ml), thus identi-
fying higher-risk subgroups with cTnI concentra-
tions at the upper end of the 99th percentile.
Large prospective studies to confirm the safety of
ED discharge with deferral of functional or
anatomic cardiac testing among low-risk subgroups
are needed.
ADDRESS FOR CORRESPONDENCE: Dr. Dustin G.
Mark, Department of Emergency Medicine, Kaiser
Permanente, 275 West MacArthur Boulevard, Oakland,
California 94611. E-mail: Dustin.G.Mark@kp.org.
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KEY WORDS acute coronary syndrome,
myocardial ischemia, risk stratification
APPENDIX For an expanded Methods section
as well as supplemental tables and a figure,
please see the online version of this article.
Mark et al. J A C C V O L . 7 1 , N O . 6 , 2 0 1 8
Comparing the EDACS and Modified HEART Score F E B R U A R Y 1 3 , 2 0 1 8 : 6 0 6 – 1 6
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